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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62006Generated: October 29, 2026

Methylamine → HCID 68701570, compound

https://huagongshe.com/reaction/62006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68702337HCID 68702337—
Reactant1-[3,4-Bis(benzyloxy)-5-nitrophenyl]-2-bromoethan-1-oneHCID 71445790—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 68701570HCID 68701570—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of methylamine (0.63 mL, 33% EtOH solution, 5 mmol) in a mixture of ethanol (25 mL) and acetic acid (0.5 mL) at room temperature was added ethyl 3-oxo-3-(2-(trifluoromethyl)pyridin-3-yl)propanoate (1.305 g, 5 mmol). The reaction mixture was heated at reflux for two hours whereupon the solvent was removed by evaporation under vacuum. To a solution of the crude product in dimethylformamide (25 mL) was added potassium carbonate (2.07 g, 15 mmol) in one portion followed by 1-(3,4-bis-benzyloxy-5-nitrophenyl)-2-bromo-ethanone (2.51 g, 5.50 mmol) and the mixture was then stirred at 100° C. Once no starting material was detectable, the reaction mixture was allowed to cool to room temperature and poured onto ice-cold 1 N aqueous hydrochloric acid (100 mL). The resulting precipitate was filtered off, washed with water and dried. The residue was chromatographed over silica gel. Homogeneous fractions were pooled and evaporated to give ethyl 5-(3,4-bis(benzyloxy)-5-nitrophenyl)-1-methyl-2-(2-(trifluoromethyl)pyridin-3-yl)-1H-pyrrole-3-carboxylate, 2.492 g (79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446012B2
Source datasetuspto-grants-2016_09
ORD IDord-4bbcba62b55541e6a17091b2f8a8fad4
Source noteuspto-grants-2016_09